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FDA 510(k)

DYNATRON 200 MICROCURRENT

K-Number: K903577 · 1991-03-15

ApplicantDynatronics Corp.
Decision Date1991-03-15
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DYNATRON 200 MICROCURRENT is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Corp.. It received FDA 510(k) clearance on 1991-03-15 under 510(k) number K903577. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNATRON 200 MICROCURRENT?

DYNATRON 200 MICROCURRENT is a medical device that received FDA 510(k) clearance on 1991-03-15. The listed applicant is Dynatronics Corp.. The 510(k) number is K903577.

When did DYNATRON 200 MICROCURRENT receive FDA 510(k) clearance?

DYNATRON 200 MICROCURRENT received FDA 510(k) clearance on 1991-03-15, under 510(k) number K903577.

Who is the listed applicant for DYNATRON 200 MICROCURRENT?

The FDA 510(k) record lists Dynatronics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DYNATRON 200 MICROCURRENT?

The FDA product code for DYNATRON 200 MICROCURRENT is GZJ.

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Other records listing Dynatronics Corp. as applicant

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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